DC30-126 TechVision Carestream Integration Operator Manual - J

Models QG-TV-F, QG-TV-IP-F,
QG-TV-C, QG-TV-IP-C,
QG-TV-F-M, QG-TV-IP-F-M,
QG-TV-C-M, QG-TV-IP-C-M
TechVision Remote Control

Panel for Quantum/Carestream
Integration System QG-DIG-DRX
Operator’s Manual
Manual Part No. DC30-126 Revision J

THE ORIGINAL VERSION OF THIS MANUAL DATED 2011-01-28 (JANUARY 28,
2011) HAS BEEN DRAFTED IN THE ENGLISH LANGUAGE BY CARESTREAM
HEALTH, INC.
This manual is copyrighted and all rights are reserved. No portion of this document
may be copied, photocopied, reproduced, translated, or reduced to any electronic
medium or machine readable form without prior consent in writing from Carestream
Health, Inc.
© Carestream Health, Inc.,2016
Carestream Health, Inc.

150 Verona Street, Rochester,NY14608, USA
www.carestream.com
Revision History
REVISION DATE TYPE OF MODIFICATION
A 2011-01-28 Initial Release ECO 2456
B 2011-08-24 Incorporated ECO 2481
C 2012-03-22 Changed EU Representative
D 2012-05-17 IEC 60601-1:2005
E 2012-08-16 Incorporated ECO 2669
F 2013-11-14 Added RS-590 fault descriptions.
G 2014-06-10 Incorporated ECO 3076
H 2015-06-22 Incorporated ECO 3522
J 2016-07-12 Updated manufacturer’s information, and deleted war-

ranty chapter
Page Page Page

Number Rev Number Rev Number Rev
i - iv J
1-1 thru 1-14 J
2-1 thru 2-8 J
3-1 thru 3-32 J
4-1 thru 4-10 J
TechVision Control Panel - Operator’s Manual Revision J

Carestream Health, Inc i
Revision History
THIS PAGE INTENTIONALLY LEFT BLANK
Revision J TechVision Control Panel - Operator’s Manual

ii Carestream Health, Inc
Table of Contents
CHAPTER 1 - SAFETY NOTICES

GENERAL SAFETY INFORMATION ......................................................... 1-3
WARNINGS, CAUTIONS, NOTES ............................................................ 1-3
REGULATORY COMPLIANCE .................................................................. 1-5
IMPORTER FOR EUROPEAN UNION ................................................. 1-6
COMPATIBILITY ............................................................................. 1-6
INTENDED OPERATOR ................................................................... 1-6
TRAINING .. ................................................................................... 1-6
ACCOMPANYING DOCUMENTATION ................................................ 1-7
APPLICABLE STANDARDS ............................................................... 1-7
ENVIRONMENTAL PROTECTION ............................................................ 1-7
DISPOSAL OF BATTERIES AND ACCUMULATORS
(DIRECTIVE 2006/66/EC) .............................................................. 1-7
ELECTROMAGNETIC COMPATIBILITY
(EN 60601-1-2:2007/IEC 60601-1-2:2007) ............. .............................. 1-8
ABREVIATIONS .................................................................................. 1-13
CHAPTER 2 - GENERAL INFORMATION

OVERVIEW . ......................................................................................... 2-3
KEY FEATURES .............................................................................. 2-4
INTENDED USE .............................................................................. 2-4
SPECIFICATIONS .. ............................................................................... 2-5
PHYSICAL SPECIFICATIONS ........................................................... 2-5
CONTROLS AND INDICATORS ....................................................... 2-5
Push Button Switches ............................................................... 2-5
DISPLAY SCREEN AND TOUCH PANEL ............................................. 2-5
ELECTRICAL SPECIFICATIONS ........................................................ 2-6
SYSTEM OPTIONS .......................................................................... 2-6
SYSTEM OPERATING ENVIRONMENT .............................................. 2-7
NON-OPERATING ENVIRONMENT ................................................... 2-7
MAIN COMPONENTS ............................................................................ 2-8
CHAPTER 3 - OPERATION
OVERVIEW . ......................................................................................... 3-3
GENERAL OPERATION .......................................................................... 3-3
THE TECHVISION DISPLAY SCREEN ................................................ 3-4
GENERAL OPERATION NOTES ......................................................... 3-6
STATUS ICONS/BUTTONS .............................................................. 3-7
ERROR MESSAGES ......................................................................... 3-8
TECHVISION/GENERATOR COORDINATION ................................... 3-10
OPERATING TECHVISION (Generator Mode) ........................................ 3-11
GENERATOR STATUS ICONS/MESSAGES ....................................... 3-12

Carestream Health, Inc iii
Table of Contents
MANUAL MODE EXPOSURE SETTINGS ............ ...............................3-14

AEC MODE EXPOSURE SETTINGS ..................................................3-15
STUDY MANAGEMENT MODE OPERATION .....................................3-22
TUBE SUPPORT DEVICE OPERATION .............................................3-26
Overhead Tube Crane Overlay Switches ...................................3-26
Floor-Mounted Tube Stand (Models QS-550 and QS-550-MAT)
Overlay Switches ...................................................................3-30
CHAPTER 4 - USER MAINTENANCE

OVERVIEW ... .......................................................................................4-3
USER MAINTENANCE ......................................................................4-3
Cleaning . .................................................................................4-4
OPERATOR CONFIGURABLE SYSTEM SETTINGS ......... ......................4-4
ACCESSING OPERATOR SERVICE OPTIONS ......................................4-4
Set Date Time ..........................................................................4-8

iv Caresteam Health, Inc
Chapter
1
SAFETY NOTICES
1-1
1-2
Chapter 1 Safety Notices
GENERAL SAFETY INFORMATION

Carestream products are designed to meet stringent safety standards. All medical
electrical equipment requires proper installation, operation, and maintenance (partic-
ularly with regard to safety).
It is vital that the user read, understand, note, and where applicable, strictly observe
all Warnings, Cautions, Notes and Safety markings within this document and on the
equipment, and that the user strictly follow all safety directions in this manual to help
ensure the safety of users and patients.
Every reasonable precaution has been taken during manufacture to safeguard the
health and safety of persons who will operate this equipment. The following precau-
tions must be observed at all times.
WARNINGS, CAUTIONS, NOTES
The following samples show how warnings, cautions, and notes appear in this docu-
ment. The text explains their intended use.
WARNING Indicates injury or death is possible if the

instructions are not obeyed.
Indicates that damage to equipment is possible
CAUTION if the instructions are not obeyed.
NOTE Indicates essential information that should be

read to avoid incorrect operation.
The purpose of safety icons, such as those shown below, is to indicate at a glance the
type of caution, warning or danger.
WARNING Ionizing radiation: indicates the possibility of

increased levels of radiation.
WARNING Dangerous voltage: indicates the presence of high

voltage.
WARNING Warning, hot surface.

Carestream Health, Inc 1-3
WARNING
Carestream disclaims all responsibility from any injury resulting from
improper application of this equipment.
This equipment is sold to be used exclusively under the prescribed direc-
tion of a person who is licensed by law to operate equipment of this nature.
This equipment must be used in accordance with all safety procedures
described in this manual and must not be used for purposes other than
those described herein. In the United States, Federal law restricts this
device to sale, distribution, and use by or on order of a licensed physician.
Carestream cannot assume responsibility for any malfunctioning of this
equipment resulting from improper operation, maintenance, or repair, or
from damage or modification of its components.
Failure to observe these warnings may cause serious injuries.
WARNING
X-rays are hazardous to both patient and operator unless established safe
exposure factors and operating instructions are observed.
Only qualified and authorized personnel shall operate this system. In this
context, qualified means those legally permitted to operate this equipment
in the jurisdiction in which the equipment is being used, and authorized
means those authorized by the authority controlling the use of the equip-
ment. Full use must be made of all radiation protection features, devices,
systems, procedures and accessories.
It is important that everyone having anything to do with x-radiation be
properly trained and fully acquainted with the recommendations of the
National Council on Radiation Protection and Measurements as published
in NCRP Reports available from NCRP Publications, 7910 Woodmont Ave-
nue, Suite 800, Bethesda, Maryland 20814-3095 (www.ncrp.com), and of
the International Commission on Radiological Protection (www.icrp.org),
and take adequate steps to protect against injury.

1-4 Carestream Health, Inc
WARNING
X-ray equipment may cause injury if used improperly. The instructions con-
tained in this manual must be read and followed when operating this unit.
Personal radiation monitoring and protective devices are available. You are
urged to use them to protect against unnecessary X-ray exposure.
REGULATORY COMPLIANCE
This certified Carestream Health, Inc medical device has been designed, manufac-
tured, and calibrated to comply with governing Federal Regulations 21 CFR Subchap-
ter J and the performance standards attendant thereto. Upon installation, all certified
products require the filing of Form FD-2579 "Report of Assembly of a Diagnostic X-ray
System" by the assembler (i.e., the installer) with the appropriate agencies; the
"Installation Quality Assurance Checklist" must also be completed and properly dis-
tributed upon installation. A copy of each form (pink copy) is provided to the user.
The installation report is completed by the installer and returned to Carestream
Health, Inc.
Those responsible for the planning of X-ray equipment installations must be thor-
oughly familiar and comply completely with NCRP Report No. 49, "Structural Shielding
Design and Evaluation for Medical Use of X-rays and Gamma Rays of Energies up to
10 MeV", as revised or replaced in the future. Those authorized to operate, test, par-
ticipate in or supervise the operation of the equipment must be thoroughly familiar
and comply completely with the currently established safe exposure factors and pro-
cedures described in publications such as Subchapter J of Title 21 of the Code of Fed-
eral Regulations, "Diagnostic X-ray Systems and Their Major Components," and NCRP
Report No. 102, “Medical X-ray, Electron Beam and Gamma Ray Protection for Ener-
gies Up to 50 MeV—Equipment Design and Use” as revised or replaced in the future.
This equipment must only be used in rooms that comply with all applicable laws or
regulations that have the force of law, concerning electrical safety for this type of
equipment.
Scheduled maintenance is essential to the assurance of continued integrity of this
equipment with respect to regulatory compliance. The continuance of certified perfor-
mance to the regulatory standard is incumbent upon the user's diligent conformance
to recommended maintenance instructions. Do not use this equipment until you are
sure that the planned maintenance program is up to date.
Complies with FDA Center for Devices and Radiological Health (CDRH) - Title 21 CFR
Subchapter J, and EC Directive 93/42/EEC for Medical Devices.
EU Authorized Representative:
Carestream Health France
1, rue Galilée
93192 NOISY-LE-GRAND CEDEX
France

IMPORTER FOR EUROPEAN UNION

Carestream Health Netherlands B.V.
Bramenberg 12
3755 BZ Eemnes
The Netherlands
The following symbols may be used for marking on this equipment or equipment
documentation:
Attention, consult accompanying

Earth (ground) documents
Protective Earth (ground) Non-ionizing radiation
Ionizing radiation Consult operating instructions
COMPATIBILITY
The equipment described in this manual must only be used in combination with
other equipment or components if these are expressly recognized by Carestream
Health, Inc as compatible.
INTENDED OPERATOR
This equipment is intended to be installed, used and operated only in accordance
with the safety procedures given within this manual for the purpose for which it
was designed. Before attempting to work with this equipment, read, understand,
note and strictly observe all warnings, cautions and safety markings on the equip-
ment.
Users include those persons who actually handle the equipment and those who
have authority over the equipment.
TRAINING
Users of this equipment shall have received adequate training on its safe and
effective use before attempting to work with the equipment. Training require-
ments may vary from country to country. The User shall make sure that training
is received in accordance with local laws or regulations that have the force of law.

ACCOMPANYING DOCUMENTATION
The documentation consists of a User manual (this document) and related docu-
mentation:
• Service Manual P/N DC30-049: Contains technical and service documentation
for this product, including installation and configuration instructions to be
performed by qualified persons.
The documentation shall be kept with the system for easy reference.
APPLICABLE STANDARDS
This equipment complies with the following regulatory standards:
• IEC 60601–1:2005—Medical Electrical Equipment—Part 1: General
requirements for safety and essential performance
• EN 60601–1:2006—Medical Electrical Equipment—Part 1: General
• CAN/CSA C22.2 No. 60601–1–08—Medical Electrical Equipment—Part 1:
General requirements for safety and essential performance
• ANSI/AAMI ES60601–1:2005—Medical Electrical Equipment—Part 1: General
MEDICAL ELECTRICAL EQUIPMENT

CONFORMS TO IEC 60601-1 AND
CERTIFIED TO CAN/CSA C22.2 NO.601.1
ENVIRONMENTAL PROTECTION
This equipment contains certain materials and chemical compounds incidental to the
manufacture of electrical and electronic equipment, and improper "end-of-life" dis-
posal of such equipment can result in environmental contamination. Therefore, this
equipment should not be disposed of as ordinary household waste, but should instead
be delivered to a designated electrical and electronic waste disposal or recycling cen-
ter. For further information on disposing of electrical and electronic waste, contact
the cognizant authority within the jurisdiction.
DISPOSAL OF BATTERIES AND ACCUMULATORS (DIRECTIVE 2006/66/EC)
In accordance with the European Directive 2006/66/EC, bat-
teries and accumulators are labeled to indicate that they are
to be collected separately and recycled at end of life. The
label on the battery may also include a chemical symbol for
the metal concerned in the battery (Pb for lead, Hg for mer-
cury and Cd for cadmium). Users of batteries and accumula-
tors must not dispose of batteries and accumulators as
unsorted municipal waste, but use the collection framework

available to customers for the return, recycling, and treatment of batteries and
accumulators. Participation is important to minimize any potential effects of bat-
teries and accumulators on the environment and human health due to the poten-
tial presence of hazardous substances.
ELECTROMAGNETIC COMPATIBILITY (EN 60601-1-2:2007/IEC 60601-

1-2:2007)
TechVision is intended for use in the electromagnetic environment specified below.
As such, TechVision must be installed and put into service according to the informa-
tion provided in the accompanying Service Manual.
Portable and mobile RF communications equipment can affect medical electrical
equipment. It is therefore recommended that the operation of equipment of this
type, such as mobile telephones, cordless microphones and other similar mobile radio
equipment, be restricted from the vicinity of this device.
Use of accessories, transducers and cables, other than those specified in the accom-
panying documents, may result in increased emissions or decreased immunity of the
equipment.
Guidance and manufacturer's declaration - electromagnetic emissions
The HF Series of X-ray generators (including TechVision option) are intended for use in the
electromagnetic environment specified below. The customer or the user of HF Series of X-ray
generators (including TechVision option) should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment -
guidance
RF emissions Group 1 The HF Series of X-ray generators

CISPR 11 (including TechVision option) use RF
energy only for their internal func-
tions. Therefore, the RF emissions
are very low and are not likely to
cause any interference in nearby
electronic equipment.
RF emissions Class A The HF Series of X-ray generators

CISPR 11 (including TechVision option) is suit-
able for use in all establishments
Harmonic emissions Class A other than domestic and those
IEC 61000-3-2 directly connected to the public low-
Voltage fluctuations/ Complies voltage power supply network that
flicker emissions supplies buildings used for domestic
IEC 61000-3-3 purposes.

Guidance and manufacturer's declaration - electromagnetic immunity
The HF Series of X-ray generators (including TechVision option) are intended for use in the electromagnetic envi-
ronment specified below. The customer or the user of the HF Series of X-ray generators (including TechVision
option) should assure that it is used in such an environment.
Immunity test IEC 60601 Compliance Electromagnetic environment
test level level - guidance
Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete

discharge (ESD) ±8 kV air ±8 kV air or ceramic tile. If floors are cov-
IEC 61000-4-2 ered with synthetic material, the
relative humidity should be at
least 30 %.
Electrical fast ±2 kV for power supply ±2 kV for power supply Mains power quality should be
transient/burst lines lines that of a typical commercial or
IEC 61000-4-4 ±1 kV for input/output ±1 kV for input/output hospital environment.
lines lines
Surge ±1 kV differential mode ±1 kV differential mode Mains power quality should be

IEC 61000-4-5 ±2 kV common mode ±2 kV common mode that of a typical commercial or
hospital environment.
Voltage dips, < 5 % UT < 5 % UT Mains power quality should be

short interruption, (>95 % dip in UT) (>95 % dip in UT) that of a typical commercial or
and voltage for 0.5 cycle for 0.5 cycle hospital environment. If the user
variations on power of the HF Series of X-ray genera-
supply 40 % UT 40 % UT tors (including TechVision option)
input lines requires continued operation dur-
(60 % dip in UT) (60 % dip in UT)
IEC 60601-4-11 ing power mains interruptions, it is
for 5 cycles for 5 cycles recommended that the HF Series
of X-ray generators (including
70 % UT 70 % UT TechVision option) be powered
(30 % dip in UT) (30 % dip in UT) from an uninterruptible power
< 5 % UT < 5 % UT supply or battery.
(> 95 % dip in UT) (> 95 % dip in UT)
for 5 s for 5 s
Power frequency 3 A/m 3 A/m Power frequency magnetic fields

(50/60 Hz) should be at levels characteristic
IEC 61000-4-8 of a typical location in a typical
commercial or hospital environ-
ment
NOTE: UT is the A.C. mains voltage prior to application of the test level.

The HF Series of X-raygenerators (including TechVision option) are intended for use in the electromagnetic
environment specified below. The customer or the user of the HF Series of X-ray generators (including
TechVision option) should assure that it is used in such an environment.
Immunity test IEC 60601 Compliance Electromagnetic environment -
test level level guidance
Portable and mobile RF communications

equipment should be used no closer to any
part of the Model 006, including cables,
than the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance
Conducted RF 3 Vrms 3 V rms

IEC 61000-4-6 150 kHz to 80 MHz d = 1,2 P
Radiated RF 3 V/m 3 V/m

IEC 61000-4-3 80 MHz to 2,5 GHz d = 1,2 P , 80 MHz to 800 MHz
d = 2,3 P , 800 MHz to 2,5 GHz
where P is the maximum output power

rating of the transmitter in watts (W)
according to the transmitter manufacturer
and d is the recommended separation dis-
tance in metres (m).
Field strengths from fixed RF transmitters,

as determined by an electromagnetic site
surveya, should be less than the compli-
ance level in each frequency range.b
Interference may occur in the vicinity of
equipment marked with the following sym-
bol:

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones
and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the measured field strength in the location in which
the HF Series of X-ray generators (including TechVision option) is used exceeds the applicable RF compli-
ance level above, the HF Series of X-ray generators (including TechVision option) should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as re-orienting or relocating the HF Series of X-ray generators (including TechVision option).
b
Over the frequency range 150 kHz to 80 kHz, field strengths should be less than 3 V/m.

Recommended separation distances between

portable and mobile RF communications equipment and the
HF Series of X-ray generators (including TechVision option)
The HF Series of X-ray generators (including TechVision option) are intended for use in an electromag-
netic environment in which radiated RF disturbances are controlled. The customer or the user of the HF
Series of X-ray generators (including TechVision option) can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmit-
ters) and the HF Series of X-ray generators (including TechVision option) as recommended below,
according to the maximum output power of the communications equipment.
Rated maximum output Separation distance according to frequency of transmitter
power of transmitter m
W
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
d = 1,2 P d = 1,2 P d = 2,3 P
0,01 0,12 0,12 0,23
0,1 0,38 0,38 0,73
1 1,2 1,2 2,3
10 3,8 3,8 7,3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation dis-
tance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter,
where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.

ABREVIATIONS
°C Degrees Celsius
A/m Amperes per meter
AEC Automatic Exposure Control
APR Anatomical Programmed Region
CCW Counter Clockwise
Cd Cadmium
CISPR International special committee on Radio Interference*
cm Centimeters
CR Computed Radiography
CSA Canadian Standards Association
CW Clockwise
DR Digital Receptor
ESD Electrostatic Discharge
GHz Gigahertz
Hg Mercury
hPa Hectopascal
IEC International Electronic Commission
kVp Tube voltage (kilovolt peak)
Ma Tube current (milliampere)
mAs Time-current product
MHz Megahertz
OCP Operator Control Panel
Pb Lead
RF Radio Frequency
SID Source Image Receptor Distance
UT A.C. mains voltage prior to application of test level
Vrms Average DC voltage
W Watts
* Note: French to English Translation for Comite’ International Spe’cial des

perturbations Radioe’lectriques


Chapter
2
GENERAL
INFORMATION
2-1
2-2
Chapter 2 General Information
OVERVIEW
NOTE: The user should read this manual in its

entirety prior to using this equipment. It should
be kept in a location near the equipment and be
readily accessible to those who operate it.
This document is intended to assist users in the safe and effective operation of the
equipment described herein. Pay special attention to all the information described in
the Safety section (refer to Chapter 1, SAFETY NOTICES).
This manual is written for trained users of the TechVision option associated with the
HF Series X-ray Generator, hereinafter referred to as the TechVision, and for autho-
rized field service personnel. Carestream Health, Inc assumes no liability for use of
this document if any unauthorized changes to the content or format have been made.
TechVision is a device that replaces the standard equipment hand grip on certain
model Carestream tube supports and is a combination of:
• a hand grip with tube stand position controls and indicators
• a generator remote control panel
• a remote control panel for a digital radiographic (DR or CR) system
TechVision is available in the following models:
• Model QG-TV-C: Replaces the standard equipment hand grips on Carestream
Model RS-590 Overhead Tube Crane System
• Model QG-TV-IP-C: Similar to Model QG-TV-C, but also has image preview
capability, and is compatible with Model RS-590 Overhead Tube Crane
System.
• Model QG-TV-F: Replaces the standard equipment hand grips on Carestream
Model QS-550 Free-Standing Tube Stand
• Model QG-TV-IP-F: Similar to Model QG-TV-F, but also has image preview
capability
• Model QG-TV-C-M: Replaces the standard equipment hand grips on
Carestream Model RS-590-MAT Overhead Tube Crane System (with Auto-
tracking option)
• Model QG-TV-IP-C-M: Similar to Model QG-TV-C-M, but also has image
preview capability, and is compatible with Model RS-590-MAT Overhead
Tube Crane System (with Auto-tracking option)
• Model QG-TV-F-M: Replaces the standard equipment hand grips on
Carestream Model QS-550-MAT Free-Standing Tube Stand (with Auto-
tracking option)

• Model QG-TV-IP-F-M: Similar to Model QG-TV-F-M, but also has image

preview capability, and is compatible with Model QS-550-MAT Free-Standing
Tube Stand (with Auto-tracking option)
All operator actions are continuously synchronized between the switches and displays
of the DR System and TechVision. X-ray PREP and/or EXPOSE are not possible from
TechVision, as these functions are done using a hard wire-connected remote hand
switch located at the Computer Workstation.
KEY FEATURES
The key features of TechVision are as follows:
• Includes physical switches that take the place of the switches on a
standard Carestream tube stand hand grip.
• Comfortable, easy-to-use hand grips.
• Remote generator control panel allows the technologist to remain close
to the patient while selecting exposure technique parameters and
managing studies.
• Incorporates a 16-bit, multi-color touchscreen, built into the hand grip
• Provides image preview and image accept/reject capability (this feature
available only on Models QG-TV-IP-C, QG-TV-IP-F, QG-TV-IP-C-M, and
QG-TV-IP-F-M).
• Models QG-TV-C-M, QG-TV-F-M, QG-TV-IP-C-M, and QG-TV-IP-F-M: Includes
motorized vertical motion up/down capability.
This product is intended to be used and operated only in accordance with the
safety procedures given within this manual for the purpose for which it was
designed. The intended use is given below. Nothing stated in this manual reduces
user's professional responsibilities for sound judgment and best practice.
INTENDED USE
The TechVision Control Panel is intended for use as a remote control device for
setting exposure and study parameters during the performance of radiographic
examinations, as well as providing all controls and indicators normally present on
the tube support device on which it is installed.
Use of the equipment for purposes other than those intended and expressly
stated by the manufacturer, as well as incorrect use or operation, may relieve the
manufacturer or his agent from all or some of the responsibility for resultant non-
compliance, damage or injury.

SPECIFICATIONS
Refer to Figure 2-1 for TechVision Remote Control Hand Grip dimensions. TechVision
Remote Control Hand Grip Specifications are as follows:
PHYSICAL SPECIFICATIONS
Height: 35.99 cm (14.17 in.)
Width: 55.80 cm (21.97 in.)
Depth: 13.51 cm (5.32 in.)
Weight: 4.3 kg (9.5 lb)
CONTROLS AND INDICATORS
Push Button Switches:
Models QG-TV-C,
QG-TV-IP-C: Vertical lock release, Longitudinal lock release,
Angulation lock release, Transverse lock release,
All Locks release, Column rotation
Models QG-TV-C-M,
QG-TV-IP-C-M: Vertical lock release, Longitudinal lock release,
All Locks release, Column rotation, Motorized ver-
tical motion up/down
Models QG-TV-F,
QG-TV-IP-F: Vertical lock release, Longitudinal lock release,
All Locks release, Auto-Stop
Models QG-TV-F-M,
QG-TV-IP-F-M: Vertical lock release, Longitudinal lock release,
All Locks release, Column rotation, Motorized ver-
tical motion up/down
Indicators:
All Models: Tube Angle Display - Analog and Digital readout
SID Display - 102 cm (40 in.), 183 cm (72 in.)
Push Button Switch Indicator - shows active
switch when push button is pressed (see Push
Button Switches above)
Detents - Longitudinal and Transverse detents are
graphically displayed on touch screen
DISPLAY SCREEN AND TOUCH PANEL
Size (measured diagonally): 25.7 cm (10.4 in.)
Resolution: 1024 x 768
Color depth: 16 bit
Touch Screen Type 4-wire resistive

ELECTRICAL SPECIFICATIONS
NOTE: The following specifications are for the TechVision

Remote Control component only and do not apply to the
tube stand, X-ray tube or collimator. Refer to tube stand,
X-ray tube and collimator manufacturer’s documentation
for applicable specifications.
Power Requirement: +28 V (dc)/0.6 A

Power Supply Type: Provided from X-ray generator
Electrical Interfacing:
QG-TV-IP-C ,
QG-TV-IP-C-M,
QG-TV-IP-F-M RJ45 CanBus
QG-TV-IP-F 15 pin D-sub
Mode of Operation: Continuous
Display: Thin film transistor LCD
SYSTEM OPTIONS
None

SYSTEM OPERATING ENVIRONMENT
NOTE: The TechVision is not designed for use in

the presence of explosive or flammable gases as
might be found in operating rooms.
Ambient Temperature: 10–40 °C (50–104 °F)

Relative Humidity: 30–75 %, non-condensing
Atmospheric Pressure: 700–1060 hPa
NON-OPERATING ENVIRONMENT
Ambient Temperature: -18–70 °C (0–158 °F)
Relative Humidity: 20–95 %, non-condensing
Atmospheric Pressure: 500–1060 hPa
13.51 cm
5.32 in.
55.80 cm
21.97 in.
35.99 cm
14.17 in.
55.80 cm
21.97 in.
T:\Storage\Manuals\Techvision\Operator抯Manual\TECHVISION DIMENSIONS.cdr
Figure 2-1. TechVision Remote Control Panel Dimensions

MAIN COMPONENTS
TechVision Operator Touchscreen - Contains a supplementary operator control panel, which
has all generator operator controls and indicators that are resident on the primary OCP, except
PREP, and EXPOSE. All aspects of X-ray techniques can be entered at the patient location, via
the TechVision. The TechVision unit is a self-contained computer, running generator control
software, designed for table top (picture frame-style) mounting.
See Figure 2-2. The TechVision is comprised of:
1. Operator Hand Grips - Used to position the tube head assembly and contains "pinky"
switches for operation of the All Locks Release control.
2. Display Screen - Contains all generator operator controls and indicators; all aspects of
X-ray techniques are entered using the Display Screen.
3. Tube support push button controls
4. Compliance label - mounted vertically to exterior of back plate.
5. Emergency Stop Push Button - Provided on auto-tracker models only (QG-TV-C-M,
QG-TV-F-M, QG-TV-IP-C-M, and QG-TV-IP-F-M). When pressed, diagnostic source
assembly (X-ray tube) motorized vertical motion is immediately stopped by removing
power from the DC motor drive circuitry. To restore power to system, turn switch
clockwise 1/4-turn
Figure 2-2. TechVision Control Panel - Main Components

Chapter
3
OPERATION
3-1
3-2
Chapter 3 Operation
OVERVIEW
This chapter provides operational information on the following TechVision topics:
• General Operation - Common displays and methods for using TechVision.
• Generator Remote Control Operation - Use TechVision as a Remote
Control to a Carestream HF Series Generator
• Study Management - Image Preview (and Approval/Reject Functionality,
requires special licensing and proper configuration) — a feature available
only on Models QG-TV-IP-C, QG-TV-IP-C-M, QG-TV-IP-F, and QG-TV-IP-F-M
interfaced with a DR System’s Workstation Computer
• Tube Support Motion Control Operation - Using TechVision to control the
tube support
The operating instructions for the auto-tracking compatible versions of TechVision
(Models QG-TV-C-M, QG-TV-IP-C-M, QG-TV-F-M, and QG-TV-IP-F-M) described briefly in
this manual, are covered in detail in the Q-Rad System Operator Manual (DC30-091).
It is imperative that all safety instructions described in this manual be strictly adhered
to in order to ensure the safety of both patient and user.
WARNING! This equipment must be operated

with reasonable care. Manufacturer’s equipment
recommendations described in this manual must
be observed.
WARNING! Safe equipment performance requires

the attention of service personnel who are specif-
ically trained and experienced with medical x-ray
apparatus. Applicable preventive maintenance or
any repair service should be performed by these
skilled individuals. Failure to follow manufac-
turer’s or service personnel’s recommendations
may result in serious injury.
GENERAL OPERATION
TechVision has been designed to enable remote parameter setting of a Carestream HF
Series Generator from a position in close proximity to the patient, including synchroni-
zation with integration software associated with radiographic workstation applications
(integrated units only). TechVision includes a touch panel display for selecting and
viewing exposure parameters, combined with hand grips for operating the tube sup-
port device to which it is attached. As such, TechVision permits monitoring and/or set-
ting of all radiographic exposure parameters, while the operator is inside the
examination room. For instructions on using the generator system, including the gen-
erator Operator Control Panel, refer to the HF Series Operator and Service Manuals
provided with the X-ray generator.

Chapter 3 Operation
NOTE: For the purpose of this manual, the term

"Operator Control Panel" means a display that
reflects the current status of the attached X-ray
Generator, including the exposure and state infor-
mation. The Operator Control Panel software will
include the service screens needed to calibrate
and configure the Generator (password entry
required to access this).
THE TECHVISION DISPLAY SCREEN
Figure 3-1. Sample TechVision Display Screen - Landscape Orientation

Figure 3-1 is an example of the Display Screen as it would appear on TechVision
when the tube head is directed toward the table (referred to as “landscape” ori-
entation). If the tube head is rotated 90 °, as when it faces the upright wall
stand, this same screen will appear on the TechVision display in “portrait” orienta-
tion as shown in Figure 3-2.

Chapter 3 Operation
Figure 3-2. Sample TechVision Display Screen (Portrait Orientation)
NOTE: The features are same whether TechVision

is in Portrait or Landscape orientation, only the
layout is changed. The elements on the screen
rearrange for optimal readability and for logical
placement.

Chapter 3 Operation
The TechVision Display Screen is divided into eight sections:

1. Mode - Buttons on the upper left that indicate the types of display screens.
The major sections in descending order are Service, Study Management and
Generator Modes. Note that the Generator Screen type selector also shows
the current status of the generator (see Table 3-1).
2. Tube Support Status Section - This area of the screen (Landscape and Portrait
orientation) contains information pertaining to the tube support device to
which the TechVision is mounted, such as source-to-image distance (SID),
height indicators, and imagery depicting any of the icons representing the
various degrees of freedom built-in to the respective tube support device,
when selected by the Operator (refer to icons in Tables 3-3, 3-4 and 3-5 later
in this chapter). The TechVision touch screen for Models RS-590 and RS-590-
MAT tube supports are slightly different with regard to display of status infor-
mation (See Figure 3-22).
3. Anode Heat/Position - The upper portion of the screen contains fixed loca-
tions for indicators (four in landscape, and three in portrait orientation). The
left-most is always the "Anode Heat" and the others normally denote either
position or orientation information, or (in landscape orientation) time/date.
4. Generator Settings (Controls & Indicators Section) - The values displayed in
the center section and lower portion mirror the controls and indicators that
appear on the generator operator control panel.
5. AEC and Manual buttons in the designated area (vertical) provided in land-
scape orientation (Figure 3-1), and in portrait orientation, the horizontal area
just below the Generator Settings, as shown in Figure 3-2.
6. AEC Detector Section - Gives the current status of active AEC ion chamber
detectors, and allows modifications to AEC detectors selected (see note
below). The field is blank when in "Manual" exposure mode.
7. Receptor (Workspace) Selection - Wall, Table, None, and AUX buttons
allows selection of the desired image receptor location (group) for the current
procedure. Where more than one "named workspace" exists, repeated actu-
ation of the Workspace button will cause the named workspace associated
with that group to be called, and the workspace name displayed above the
button to show it is current.
8. Patient and Study Information - Data from the DR System’s Workstation Com-
puter that identifies the patient and the name of the procedure being per-
formed (blank when no patient is selected). Note that the selected procedure
is shown in the top portion of the window, while the patient data is shown
below.
GENERAL OPERATION NOTES
The current time and date are generally displayed in the upper right corner of the
TechVision Display Screen when in Landscape orientation. Note that changing the
time elsewhere in the system will not affect this display, since the time and date
settings for TechVision are made within TechVision service mode.

Chapter 3 Operation
All Techvision Control Panel buttons are gray when not selected, and are yellow
when selected.
Pressing the increment or decrement arrows (left) below the exposure
parameter (i.e., KVP, MA, and Time/MAS) will increase or decrease the
respective parameter within the limits set by the generator. At all times
when the buttons are not depressed, the generator OCP display will be
synchronized with the TechVision display.
The AEC adjustment buttons show the current setting of the exposure modifica-
tion values (i.e., AEC Density). Their legend and present values are shown above
the respective button. If the modification value is changed on another generator
OCP screen, it will be reflected on the TechVision display.
Any error messages from the generator and other sources are indicated by
an "ATTENTION" icon (left), which when tapped, opens a dialog box con-
taining an explanation. The PREP and EXPOSE functions are inhibited dur-
ing periods when the system is in its error state.
TechVision will display "System Offline" over a blank field, in the event that Ether-
net communications is lost, the Network is not operational, or an IP Address prob-
lem is present in the System.
When the generator is ready to take an exposure, the "Generator Ready" message
is displayed on the TechVision Display Screen, immediately above the radiation
icon.
When the "Prep" button is pressed (a hand-held switch mounted in near proximity
to the generator operator control panel), a gray X-ray radiation symbol briefly
appears in the generator status area (section 1, Figures 3-1 and 3-2), followed by
a green "Prepped" radiation symbol. Similarly, when the "Expose" button is
pressed, a yellow "Expose" radiation symbol appears in the generator status area.
See Table 3-2 for a directory of generator icons.
STATUS ICONS/BUTTONS
The three buttons in the upper left region of the landscape or portrait screen are
used to select Service Mode, Study Management Mode, or Generator Mode when
using TechVision (see Table 3-1).
Table 3-1: Operating Mode Icons
Status Icon Controls

Service Mode: Includes operator and service option setting for the
TechVision. Always the same image. Double tap to enter Service Mode.
Study Management Mode: Indicates status (OK or Not Connected)

of the Study Management system. Touch to make Study Management
the main content of the screen.

Chapter 3 Operation
Table 3-1: Operating Mode Icons
Status Icon Controls

Generator Mode: Indicates the generator status (See Generator Sta-
tus Icons shown in Table 3-2). Touch to make Generator Control the
main content of the screen.
ERROR MESSAGES
When the X-ray generator will not initiate an exposure, an audible alert will sound
and an "Attention" icon will appear on TechVision display screens in place of the
Generator Status icon (see Figure 3-3). All Prep and Expose activities will be
inhibited and/or terminated.
In order to understand the error that caused the "ATTENTION" icon to be dis-
played, touch the button and a dialog box with the error will appear (see Figure
3-4).
ATTENTION
ICON
Figure 3-3. TechVision Generator Screen (Error Status)

Chapter 3 Operation
TOUCH ICON
TO READ
ERROR
MESSAGE
Figure 3-4. TechVision Generator Screen (Error Message Dialog)

Touch OK to attempt to clear the error indication and get the Generator back into
the condition where a "Generator Ready" indication is displayed. Note that resto-
ration of the Generator could take a few moments. An error that has not been
successfully corrected will reappear when the triggering event occurs again. For
example: If an error is not successfully corrected, an attempt to Prep the Gener-
ator will result in the System registering the same error.
NOTE: Refer to the HF Series X-ray Generator Ser-

vice Manual and/or the appropriate tube stand or
other tube support device manual for descriptions
and assistance in interpreting error messages.
Certain errors can be resolved by the operator,
while others require technical assistance.

Chapter 3 Operation
TECHVISION/GENERATOR COORDINATION
As long as TechVision and generator console are successfully connected, both
units will remain synchronized, without regard to which unit was used for user
input.
GENERATOR
CONTROL
PANEL
Figure 3-5. &DUHVWUHDP Q-Rad Generator Control Panel Integrated with CR/DR
System’s Workstation Computer

Chapter 3 Operation
Figure 3-6. Example of Exposure Parameter Settings

Arranged for Display on TechVision
As shown in Figures 3-5 and 3-6, the TechVision touch screen displays the same
information as the generator control panel console, however the information is
arranged to accommodate the size and shape of the TechVision display screen.
NOTE: Whether the selection is made on

Workstation Computer or TechVision, the selected
button turns yellow on the TechVision Display
Screen.
If any exposure buttons on the connected Generator Control Panel are manipu-
lated, the TechVision display changes to correspond to that setting, and vice-
versa.
OPERATING TECHVISION (GENERATOR MODE)

The following paragraphs describe operation of the TechVision control panel in "Gen-
erator Mode", and how the operator can determine Generator status from the TechVi-
sion display.
Most of the TechVision's generator control functions are very similar or identical to
those appearing on the associated generator control panel display. Therefore, this
manual focuses primarily on explaining the functions that are presented differently on
TechVision as compared to those presented on the Generator Control Panel. Refer to
the appropriate generator or integration system operator's manual for complete
instructions on setting generator exposure parameters.

Chapter 3 Operation
GENERATOR STATUS ICONS/MESSAGES

Figure 3-7 shows the TechVision touch screen display in Landscape orientation.
The "Generator Ready" message is called-out on the left side of the display just
above the button containing the radiation symbol. The radiation symbol is both
an indicator and a dynamic control button, which when touched, allows the Oper-
ator to enter the Generator mode for programming. Table 3-2 shows the icons/
messages that could be displayed on the TechVision touch screen.
NOTE: Identical Generator status icons/messages

(except "Disconnected") are shown on the associ-
ated Workstation Computer’s Generator Control
Panel screen. These corresponding icon/message
displays cease when TechVision is disconnected.
GENERATOR
READY MESSAGE
INDICATES THAT
THE GENERATOR
IS READY FOR
OPERATION
Figure 3-7. TechVision Touch Screen Display - Generator Status Icon
Table 3-2: Generator Status List
INDICATION DESCRIPTION
Disconnected Indicates that the Workstation Computer is not communicating with

the Q-Rad Generator.
Ready Indicates that the Generator is communicating with the Workstation

Computer and is ready for an exposure.

Chapter 3 Operation
Table 3-2: Generator Status List
INDICATION DESCRIPTION
In the process of readying the Generator to begin an exposure.

The Prepping icon is revealed during the cycle. A transition from
the radiation icon (far left) to the Prepping icon (near left) occurs
Radiation
Icon
Prepping
Icon
prior to presentation of the "Prepped" icon (see below).
Prepping
The Generator is ready to accept an expose command.
Prepped
The Generator is emitting radiation.
Expose
Charging Indicates that the Generator is incapable of making an exposure,

and the batteries are charging (Stored Energy Generators only).
File Access Indicates that the Generator is in the process of acquiring opera-
tional data from an independent file or a peripheral.
Recovery Indicates that the Generator is connected, but not ready. Can also
indicate that data is being acquired, or an equipment process cycle
is taking place.
Off Indicates that power to the Generator is in STANDBY. This is dis-

played when the Generator enters its automatic energy conserva-
tion mode. It will also be displayed if a power failure occurs, or if
the Generator’s Power/Expose Control Box is set to STANDBY.
Sleep Indicates that the Generator has reverted to Automatic Power

Standby Mode due to inactivity.
There is a Generator problem that is causing the need for atten-

tion. Touch the error icon to display details about the error.
Error

Chapter 3 Operation
MANUAL MODE EXPOSURE SETTINGS

Refer to Figure 3-8, and the following instructions to make Manual Mode expo-
sure settings.
NOTE: Typically, the pre-programmed procedures

include embedded control over the use of AEC or
Manual mode. The MANUAL and AEC buttons on
the TechVision display toggle the system mode
when each is touched. This allows for an override
of the pre-programmed mode selection, while the
operator is in the patient area.
PRESS HERE TO
TOGGLE BETWEEN
MAS AND TIME
UNIT DISPLAY
Figure 3-8. TechVision Display Screen (Landscape Orientation) - Manual Mode

1. Touch the MANUAL mode button on either the Workstation’s Generator Con-
trol Panel or TechVision Screen to change to the Manual (non-AEC Mode)
exposure selection. The Manual Mode screen appears on both TechVision
and the generator control panel.
2. Verify the exposure (technique) settings are correct. If necessary, modify the
technique using the KVP, MA, or MAS/TIME increment/decrement arrow
buttons as required.
3. Select the desired Workspace (Receptor).
4. Take the exposure.
5. If near the TechVision, verify the Post Time or mAS, which is selected by
touching Time/mAs (see Item 5 in figure above).

Chapter 3 Operation
AEC MODE EXPOSURE SETTINGS

Refer to Figure 3-9, and the following instructions to make AEC Mode exposure
settings.
2
8
6 5
Figure 3-9. TechVision Display Screen (Landscape Orientation) - AEC Mode

1. Touch the AEC mode button on either the Workstation Computer’s Generator
Control Panel or the TechVision Display Screen. The AEC Mode screen appears
on both TechVision and the generator control panel.
2. Verify the technique selections are correct. Modify technique settings using
the KV and MA increment/decrement buttons as required.
3. Verify AEC Density selection is correct.
4. If necessary, modify the Density setting by using the increment/decrement
arrow buttons to adjust this setting as required. Each step increases or
decreases the mAs in 15 % increments above or below the nominal density
setting (i.e., 0 %). There are a total of 11 available steps (-15, -30, -45, -60,
-75 nominal, +15, +30, +45, +60, +75).
5. Verify or select the desired ion chamber field combination using the three AEC
field buttons. When selected, the AEC Field button will turn yellow.
6. Verify or Select a Receptor.
7. Take the exposure.
8. If near the TechVision, verify the Post Time or mAs, which is selected by
touching Time/mAs (see Item 8 in figure above).

Chapter 3 Operation
OPERATING TECHVISION (STUDY MANAGEMENT MODE)

TechVision Models QG-TV-IP-C, QG-TV-IP-C-M, QG-TV-IP-F, and QG-TV-IP-F-M are
designed to integrate not only with the Carestream X-ray generator (to maintain expo-
sure setting synchronization), but also with a DR Imaging System, when applicable.
For the purpose of this discussion, the DR Imaging System will be referred to as the
"Workstation Computer".
Examination (procedure) settings displayed on the Workstation Computer’s screen are
continuously synchronized with the settings on the TechVision display screen. This
allows the operator to make exposure settings at either the Workstation Computer
screen or the TechVision screen.
Communication with a Workstation Computer provides TechVision with additional
capabilities, such as the ability to preview acquired images (if Image Preview permit is
selected in the TechVision Service Setup), and assign image accept/reject status to
images in the Patient Study (requires optional "Image Reject" functionality).
The "Study Management" icon can either be ready to display the procedures indicated
on the Workstation Computer screen, or it can indicate that it is disconnected.
Study Management: Indicates connected status of Study Manage-
ment system. Touch to make Study Management the main content of
the screen.
Study Management Disconnected: Indicates that TechVision is not
communicating with the connected DR System’s Workstation Computer.
The TechVision Study Management Mode Screen is initiated by selecting
a patient at the Workstation Computer, in accordance with the imaging system’s
operating instructions (see Figure 3-10).

Chapter 3 Operation
PATIENT NAME AND GENERATOR

IDENTIFICATION DATA CONTROL PANEL
STUDIES
PROCEDURES
Figure 3-10. Study Management -

Initiated on Imaging System’s Workstation Computer
Selecting a study and/or procedure from the Workstation Computer causes the
procedure to appear on the TechVision display.

Chapter 3 Operation
2 3 5 6
Study
Management
Button
Generator
Mode
Button
THIS PROCEDURE
IS CURRENT
TechV Gen Scr - Study Management Mode.cdr
Figure 3-11. TechVision Study Management Mode Screen - Views Display
NOTE: If a patient has not been selected, the pro-

cedure selection buttons shown above will not be
displayed.
Make sure the Study Management mode button on the TechVision screen is
selected to view the TechVision Study Management Mode Screen (see
Figure 3-11). The main TechVision Study Management Mode screen elements are
as follows:
1. Patient ID Number - Obtained from the Workstation Computer
2. Patient Name - Obtained from the Workstation Computer
3. Main Procedure area - Displays the patient’s procedures for the selected
study. The images in this area correspond with those presented on the Work-
station Computer.
4. If more than 8 images are in the study, up/down scroll arrows will appear.
Use the up/down arrows to view the previous and/or next screen containing
additional thumbnail images.
5. Study/View Information - Obtained from the Workstation Computer

Chapter 3 Operation
6. Studies button - Select to view a list of the available studies for the current
patient (defined by unique accession number as assigned by the Carestream
DRX-1 Imaging System). Pressing the Views button (see Figure 3-12 below)
returns to the Study Management Mode Screen -Views display):
THIS STUDY IS PRESS TO

CURRENT DISPLAY
PROCEDURES
(VIEWS)
Figure 3-12. TechVision Study Management Mode Screen - Studies List Display
To select a different study for this patient, touch the desired study button in the
displayed list. Once selected, the study button color changes to yellow to indi-
cate it is now current. To see the views within the study, select the Views but-
ton. The TechVision Study Management Screen (Figure 3-13) appears.
To make another procedure (view) within this study current, touch the appropri-
ate thumbnail image denoting the desired procedure. Once selected, the thumb-
nail image displays a yellow border around its perimeter (until the X-ray image is
acquired). Note that, if a procedure (thumbnail) has been designated as an
"accepted" exposure (has a green check superimposed over it), it cannot be
made current again.

Chapter 3 Operation
All generator control panel operator screens will be synchronized:

• The TechVision screen shows all images acquired, and any procedures ready for
image acquisition.
• The Generator Operator Console screen on the Workstation Computer will
display the name of the procedure (if permitted), and the exposure parameters
of that View.
• The Workstation Computer will also display the View (highlighted) and,
depending on the integration system, the exposure parameters indicated.
SELECT BETWEEN STUDY

MANAGEMENT AND
GENERATOR MODES
USING THESE BUTTONS
Figure 3-13. TechVision Study Management Mode Screen -

Procedure Views Display
Select the Study Management Mode by touching the Study button, shown below on the
TechVision touch screen.
Figure 3-14. TechVision - Study Management Mode Button

Chapter 3 Operation
To enter the Generator Mode screen, while viewing the Study Management
Screen, touch the Radiation icon beneath the Study Management button on the
TechVision d isplay.
Figure 3-15. TechVision - Generator Mode Button

This will change the display to the Generator Mode screen shown in Figure 3-.
PATIENT
NAME & ID
PROCEDURE
NAME
Figure 3-16. TechVision Generator Mode Screen|

(Patient and Procedure Information Indicated)
Note that the current exposure selection is identical on both the Workstation
Computer’s Generator Control Panel and the TechVision Generator Mode screen.
The Post Time/mAs indicators are not synchronized between the Generator Con-
trol Panel and the TechVision display in Generator mode.
The name of the procedure and patient identification is contained in the following
areas on the TechVision Generator Mode screen:
1. Procedure Name
2. Patient Name and ID

Chapter 3 Operation
Typically, the TechVision Generator Mode screen would be selected either to verify
the exposure settings, or for modification of the exposure settings while the oper-
ator is in close proximity to the patient. If exposure modification is desired, follow
the "OPERATING TECHVISION (GENERATOR MODE)" procedures described previ-
ously in this Chapter.
STUDY MANAGEMENT MODE OPERATION
As described in the previous paragraphs, the session begins with the selection of
a Patient and a series of studies/procedures that are ordered for that Patient.
This is accomplished via the DR system Workstation Computer’s touch screen
(see Figure 3-10). Upon selection of an image and verification of proper expo-
sure settings, the X-ray exposure is taken as described in the associated Integra-
tion System Operator’s Manual (P/N DC30-123).
CONTINUE BUTTON
IMMEDIATELY RESIZES
IMAGE TO THUMBNAIL
Figure 3-17. TechVision Image Preview Screen (After exposure, but before
"Continue" is pressed, or Timeout period has elapsed)
Within seconds of completing the exposure, a QA (preview) image appears (full
screen) on the TechVision, such as shown in the example in Figure 3-17. The
TechVision preview image is a re-sized version of the preview image appearing on
the associated imaging system’s workstation acquisition console. This image is
not intended to be used for medical diagnostic purposes. Preview images allow
the operator, from a location close to the patient, to determine if acceptable posi-
tioning, exposure settings, etc., were achieved.
After the TechVision Image Preview Screen is displayed, the image "times out"
after a preset time if no action is taken. When this occurs, the preview image
reverts to a thumbnail view of the image on the Study Management Mode screen,

Chapter 3 Operation
Depending on how the system may be configured, the time-out function may be
disabled, in which case the Preview Screen will remain displayed until a screen
button is pressed (Note: The time-out period is configurable, but can only be set
by a Service Technician). Present on the right side panel of the TechVision Image
Preview Screen is an area specifically used for disposition of the acquired image.
A Continue button (all systems) and, if this system is configured with optional
Image Accept and Reject functionality, Accept and Reject buttons will be dis-
played. The following describes the function of each button:
• If "Accept" functionality is configured, selecting Accept communicates
back to the Workstation Computer "image acceptance". The TechVision
returns to the Study Management Mode screen and advances to the next
procedure icon, indicated by a yellow border surrounding it. The
accepted exposure is indicated by a green "check mark" superimposed
over the image thumbnail, as shown below.
THIS PROCEDURE
IS CURRENT
Figure 3-18. Sample TechVision Study Management Screen

(Accepted Image)
• If "Reject" functionality is configured, selecting Reject communicates
back to the Workstation Computer "image rejection". A Reject Reason
Screen is then displayed as shown in the sample screen below. Select

Chapter 3 Operation
the appropriate reason for rejecting the image. The system returns to
the Study Management Mode screen and automatically creates and re-
selects the same procedure icon for a retake of the image.
REJECT
BUTTON
Figure 3-19. TechVision Image Reject Reason Screen

(Superimposed Over Preview Image Screen After Rejection)

Chapter 3 Operation
Select Continue to proceed with the next procedure without deciding the disposi-
tion of the last image ("accept" nor "reject") using TechVision. The Study Man-
agement Mode screen (thumbnail view) will be displayed with a yellow border
surrounding the thumbnail (i.e., no disposition (acceptance) indicated). In the
sample screen below, the image Continue button was selected.
Figure 3-20. Sample TechVision Study Management Screen

(Before Next Exposure)
Follow the previous steps to complete the remaining procedures in the study.

Chapter 3 Operation
Note that at any time during the examination, double-clicking (or double-tapping)
on a previously captured image in the Study Management Mode Screen brings up
the image full-size in the TechVision Image Preview Screen, as shown below:
Figure 3-21. Preview Screen (Previously Captured Image)

Select Continue to return to the Study Management Mode Screen.
TUBE SUPPORT DEVICE OPERATION
Movement of the tube support device (i.e., Models RS-590 and RS-590-MAT Over-
head Tube Crane or Models QS-550 and QS-550-MAT Tube Stand) is controlled
using the push-buttons on the TechVision front panel to the left and right of the
display screen. When any of these buttons is pressed, the corresponding icon is
displayed on the TechVision screen to confirm the switch has been depressed.
A functional description of switches for each tube support device is provided in
the following paragraphs. The operating instructions for the auto-tracking com-
patible versions of TechVision (Models QG-TV-C-M, QG-TV-IP-C-M, QG-TV-F-M, and
QG-TV-IP-F-M) described briefly in this manual, are covered in detail in the Q-Rad
System Operator Manual (DC30-091). The descriptions cover only the actions of
the tube support devices that are affected by the TechVision. In order to fully
understand all tube support device motions and control limitations, the tube sup-
port operation instructions provided in this manual must be read in conjunction
with the tube support device Operator's Manual.

Chapter 3 Operation
Overhead Tube Crane Overlay Switches

Figure 3-22depicts the various overlay switches for the TechVision
mounted on an Overhead Tube Crane tube support device. Table 3-3
explains the function of each TechVision overlay switch.
Figure 3-22. TechVision for Overhead Tube Crane (Motion Control Lock Button)
Table 3-3: Overhead Tube Crane Overlay Switches
Switch Icon Description Function
Floating X-ray Tube All tube motion locks released.

Unit Travel (Note: The buttons on the hand grip handles also
activate this function.)
Horizontal 90 ° (Wall Releases the X-ray tube angle lock to enable vertical
Stand) X-ray Tube rotation.
Unit or oblique
exposure (0 ° and
±90 °) Lock-in Posi-
tions

Chapter 3 Operation
Longitudinal X-ray Releases the longitudinal lock allowing the tube

Tube Unit Travel crane structure to move parallel to patient position-
ing table or film-focus distance from wall stand.
The icon shown at left is displayed on the TechVision

touch screen (Overhead Tube Crane application)
when the longitudinal trolley is at its detent point.
Rotate X-ray Tube Allows the X-ray tube to be rotated about its vertical
Unit around vertical axis.
axis
Vertical X-ray Tube Releases the X-ray tube unit vertical motion lock.
Unit Travel
Model RS-590-MAT When this button is pressed, motorized vertical

only - Motorized Ver- motion of the diagnostic source assembly (X-ray
tical Motion Up tube) in the upward direction is activated, Upward
push-button switch motorized motion is disabled when this switch is
released.
Model RS-590-MAT When this button is pressed, motorized vertical

only - Motorized Ver- motion of the diagnostic source assembly (X-ray
tical Motion Down tube) in the downward direction is activated, Down-
push-button switch ward motorized motion is disabled when this switch
is released.
Transverse X-ray Release the X-ray tube transverse locks so the struc-
Tube Unit Travel ture can move across the
positioning table.
The icon shown at left is displayed on the TechVision

touch screen (Overhead Tube Crane application)
when the Transverse trolley is at its detent point.

Chapter 3 Operation
Tube stand motion Displayed when motion system is enabled and ready
control system lock for axis movement. Toggles between "Locked" and
status indicator "Unlocked". This icon is active only during periods
("Unlocked") when the motion system is not being operated. Oth-
erwise, the appropriate motion icon is displayed.
Tube stand motion Displayed when the motion system is disabled, and
control system lock not permitted to move. Toggles between "Locked"
status ("Locked") and "Unlocked". Any attempt to operate the motion
buttons will result in a fault.
Fault in Tube stand Displayed when axis movement is attempted while

motion control sys- the tube stand motion control system is in locked
tem lock status condition.
Tap this icon, to unlock the axes.
Fault in collimator Displayed when the collimator fails to properly com-

RS-590 communications on municate over CAN bus with TechVision and worksta-
Collimator
the CAN bus tion.
+
Fault in communica- Displayed on TechVision Screen, when tube support

RS-590 tions to or from the fails to properly communicate with its interface
Disconnected
motion system board.
+
Fault in internal Displayed on TechVision screen when the System is

RS-590 communications of disabled due to communication failure(s) within the
Internal Comm
the tube support mechanical system.
+

Chapter 3 Operation
Floor-Mounted Tube Stand (Models QS-550 and QS-550-MAT)

Overlay Switches
Figure 3-24 depicts the positioning push-buttons for the TechVision
mounted on a Floor-Mounted Tube Stand tube support device. Table 3-4
explains the function of each TechVision overlay switch.
ICON DISPLAYED
CORRESPONDS TO
BRAKE RELEASE
SELECTED
ROTATE
VERTICAL
ANGLE ANGLE
ALL ALL
TUBE HEAD
POSITIONAL
DEFAULT ICON
Figure 3-23. Overlay Switches - TechVision on Floor-Mounted Tube Stand
Table 3-4: Floor-Mounted Tube Stand Overlay Switches
Auto-Stop When this button is pressed along with

Longitudinal Lock Release button, longitu-
dinal movement of the vertical column
stops automatically when it reaches either
the 40 in. or 72 in. SID detent on floor
track.

Chapter 3 Operation
Vertical X-ray Releases the X-ray tube unit vertical

Tube Unit Travel motion lock.
The icon shown immediately to the left

appears on the TechVision Screen and
indicates that the vertical trolley has
reached its 40 in. SID position.
Model QS-550- When this button is pressed, motorized

MAT only - Motor- vertical motion of the diagnostic source
ized Vertical assembly (X-ray tube) in the upward
Motion Up push- direction is activated, Upward motorized
button switch motion is disabled when this switch is
released.
Model QS-550- When this button is pressed, motorized

MAT only - Motor- vertical motion of the diagnostic source
ized Vertical assembly (X-ray tube) in the downward
Motion Down direction is activated, Downward motor-
push-button ized motion is disabled when this switch is
switch released.
Rotate X-ray Tube Releases the X-ray tube angle lock to

Unit around verti- enable vertical rotation.
cal axis (Note: Activating this motion will cause
the Angle Display to appear on the Tech-
Vision screen.)
Floating X-ray All tube motion locks released.

Tube Unit Travel (Note: The buttons on the hand grip han-
dles also activate this function.)
Transverse X-ray Releases the X-ray tube transverse locks

Tube Unit Travel so the structure can move across the posi-
tioning table.

Chapter 3 Operation
Longitudinal X- Releases the longitudinal lock allowing the

ray Tube Unit tube stand structure to move parallel to
Travel patient positioning table or film-focus dis-
tance from wall stand.
The icons shown immediately to the left

appear (separately) on the TechVision
Screen and indicates that the Tube Stand
has traversed longitudinally into the
detent for either 40 in. or 72 in. SID.

Chapter
4
USER
MAINTENANCE
4-1
4-2
Chapter 4 User Maintenance
OVERVIEW
This chapter contains information to assist the system user in maintaining the smooth
operation of the TechVision Control Panel. Also included in this chapter are instruc-
tions for making changes to the system's user-configurable settings, such as setting
the date and time.
This product has been factory tested to assure its required performance in an X-ray
system.
WARNING! Failure to follow manufacturer’s or

service personnel’s recommendations may result
in serious injury.
WARNING! Only qualified and authorized persons

shall work on this equipment. In this context,
qualified means those legally permitted to work
on the equipment, and authorized means those
specifically authorized by local management.
WARNING! Changes, additions or maintenance to

the equipment carried out by persons without
appropriate qualifications and training and/or
using un approved spare parts may lead to serious
risk of injury and damage to the equipment as
well as making the warranty void.
USER MAINTENANCE
WARNING! Electric shock hazard! The TechVision

control panel contains no user serviceable compo-
nents. Do not attempt to disable these compo-
nents or remove any trim covers. Refer service to
qualified service personnel.
The user is responsible for performing certain routine maintenance and inspection
procedures. Aside from routine maintenance, any abnormal noise, vibration, or
unusual performance should be investigated by a qualified service representative.
Preventive maintenance or any repair service should be performed only by quali-
fied service personnel.
User maintenance consists of the following activities, which should be performed
on a daily basis:
• Visually inspect the TechVision control panel for wear and cleanliness.
• Clean exterior painted surfaces of the TechVision control panel.

Cleaning
WARNING! Always disconnect the equipment

from the main power supply prior to any cleaning.
NOTE: Always test cleaning and/or disinfecting

agents, such as wipes, sprays and hand sterilizers,
on a small inconspicuous area of the equipment
prior to use. Proceed with cleaning only if no dam-
age occurred to the test area.
The system user is responsible for the basic cleanliness of the equipment. On
a regular basis, the surface should be wiped clean. Painted metal surfaces
should be cleaned using a clean cloth slightly moistened in warm soapy water
(use mild soap). Wipe with a clean wet cloth, then dry. Never use abrasive
polish on this equipment.
OPERATOR CONFIGURABLE SYSTEM SETTINGS
There are several operational service options that are configurable by the user.
These options include the Time, Date, and Touch Screen Calibration. The follow-
ing paragraphs describe access to and selection of the various operator service
options.
ACCESSING OPERATOR SERVICE OPTIONS
Operator Service Options can only be performed by accessing the TechVision
Remote Control's Operator Service Mode. To gain access to the Operator Service
Mode, password entry is required. This is to prevent unintended and/or unautho-
rized changes to system settings. To access Operator Service Mode, proceed as
follows:
1. On the TechVision Display Screen,
touch twice within one second on
the Quantum Logo (shown at right).
2. Once the Operator Service Mode has
been selected, the Password Screen will appear
(see Figure 4-1).
3. Use the numeric "touch" keypad to enter the Operator Password (3497),
then press ENTER.
NOTE: The TechVision returns to the previous

screen when an incorrect password is entered, or
after 15 seconds with no button presses.

TOUCH 3 - 4 - 9 - 7,
AND THEN TOUCH
"ENTER"
Figure 4-1. Password Screen

4. Upon successful entry of the Operator Service Password, the Service Options
Menu will be displayed (see Figure 4-2).

Figure 4-2. Operator Options Menu

5. Choose either of the options shown in Figure 4-2, or press EXIT to return to
the previous screen.

6. If Calibrate Touch Screen was selected the system will allow you to re-cali-
brate the touch settings:
Figure 4-3. Calibrate Touch Screen

7. Follow the instructions on the screen in Figure 4-3. Touch and then release
the screen in manner as it will be touched under normal use. The cross hair
will move to four positions before prompting confirmation.

Figure 4-4. Calibration Confirmation Screen

8. Figure 4-4 shows the Calibration Confirmation Screen. If the calibrations per-
formed to reach the screen shown in the Figure are to be saved, tap the
screen and the new settings will be stored in permanent memory, and the
Operator Service Menu screen will appear. If no action is taken, and the
elapsed timer on the screen is allowed to finish its countdown, the new cali-
brations will be discarded, and the previous touch screen calibrations will be
restored. The TechVision will then return to the Operator Service Menu.
Set Date Time
Select Change Date Time if you wish to observe or change the current
date or time. (Note that this date / time is not synchronized with any
other calendar or clock in the system.)
Refer to Figure 4-5, and use the appropriate keys on the TechVision touch
screen, under each of the variables to set the date / time, then select
Back to return to the Operator Service Menu.

Figure 4-5. Set Date and Time Screen



DC30-126 TechVision Carestream Integration Operator Manual - J

Uploaded by

Copyright:

Available Formats

DC30-126 TechVision Carestream Integration Operator Manual - J

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

DC30-126 TechVision Carestream Integration Operator Manual - J

Uploaded by

Copyright:

Available Formats

Models QG-TV-F, QG-TV-IP-F,

TechVision Remote Control

Manual Part No. DC30-126 Revision J

© Carestream Health, Inc.,2016

Carestream Health, Inc.

REVISION DATE TYPE OF MODIFICATION

A 2011-01-28 Initial Release ECO 2456

B 2011-08-24 Incorporated ECO 2481

C 2012-03-22 Changed EU Representative

D 2012-05-17 IEC 60601-1:2005

E 2012-08-16 Incorporated ECO 2669

F 2013-11-14 Added RS-590 fault descriptions.

G 2014-06-10 Incorporated ECO 3076

H 2015-06-22 Incorporated ECO 3522

J 2016-07-12 Updated manufacturer’s information, and deleted war-

Page Page Page

1-1 thru 1-14 J

2-1 thru 2-8 J

3-1 thru 3-32 J

4-1 thru 4-10 J

TechVision Control Panel - Operator’s Manual Revision J

THIS PAGE INTENTIONALLY LEFT BLANK

Revision J TechVision Control Panel - Operator’s Manual

CHAPTER 1 - SAFETY NOTICES

CHAPTER 2 - GENERAL INFORMATION

TechVision Control Panel - Operator’s Manual Revision J

MANUAL MODE EXPOSURE SETTINGS ............ ...............................3-14

CHAPTER 4 - USER MAINTENANCE

Revision J TechVision Control Panel - Operator’s Manual

GENERAL SAFETY INFORMATION

WARNING Indicates injury or death is possible if the

NOTE Indicates essential information that should be

WARNING Ionizing radiation: indicates the possibility of

WARNING Dangerous voltage: indicates the presence of high

WARNING Warning, hot surface.

TechVision Control Panel - Operator’s Manual Revision J

Revision J TechVision Control Panel - Operator’s Manual

TechVision Control Panel - Operator’s Manual Revision J

IMPORTER FOR EUROPEAN UNION

Attention, consult accompanying

Protective Earth (ground) Non-ionizing radiation

Ionizing radiation Consult operating instructions

Revision J TechVision Control Panel - Operator’s Manual

MEDICAL ELECTRICAL EQUIPMENT

TechVision Control Panel - Operator’s Manual Revision J

ELECTROMAGNETIC COMPATIBILITY (EN 60601-1-2:2007/IEC 60601-

Guidance and manufacturer's declaration - electromagnetic emissions

RF emissions Group 1 The HF Series of X-ray generators

RF emissions Class A The HF Series of X-ray generators

Revision J TechVision Control Panel - Operator’s Manual

Guidance and manufacturer's declaration - electromagnetic immunity

Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete

Surge ±1 kV differential mode ±1 kV differential mode Mains power quality should be

Voltage dips, < 5 % UT < 5 % UT Mains power quality should be

Power frequency 3 A/m 3 A/m Power frequency magnetic fields

TechVision Control Panel - Operator’s Manual Revision J

Guidance and manufacturer's declaration - electromagnetic immunity

Portable and mobile RF communications

Recommended separation distance